The current paradigm for the identification of candidate drugs within the pharmaceutical industry typically involves the use of high throughput screens (HTS). High content screening (HCS) is the term given to the process of using an imaging platform to screen large numbers of compounds for some desirable biological activity. Classification methods have important applications in high content screening experiments where they are used to predict which compounds have the potential to be developed into new drugs. In this paper a new classification method is proposed for batches of compounds where the rule is updated sequentially using information from the classification of previous batches. This methodology accounts for the possibility that...
The file attached to this record is the author's final peer reviewed version. The Publisher's final ...
Recent technological advances in high-content screening instrumentation have increased its ease of u...
The versatility of similarity searching and quantitative structure-activity relationships to model t...
High throughput screening experiments are typically used within the pharmaceutical industry for the ...
High throughput screening experiments are typically used within the pharmaceutical industry for the ...
Modern high-throughput screening (HTS) is a well-established approach for hit finding in drug discov...
High Throughput Screening (HTS) is used in drug discovery to screen large numbers of compounds again...
Millions of compounds are available as potential drug candidates. High throughput screening (HTS) is...
High Content Screening (HCS) is a technology that allows life scientists to analyze the effect of bi...
In drug discovery, high content screening (HCS) is an imaging-based method forcell-based screening o...
Background: Computational support for high-content screening (HCS) is of paramount importance at sev...
Complex mixtures containing natural products are still an interesting source of novel drug candidate...
Modern high-throughput screening (HTS) is a well-established approach for hit finding in drug discov...
High-content screening is an empirical strategy in drug discovery toidentify substances capable of a...
Recent technological advances in high-content screening instrumentation have increased its ease of u...
The file attached to this record is the author's final peer reviewed version. The Publisher's final ...
Recent technological advances in high-content screening instrumentation have increased its ease of u...
The versatility of similarity searching and quantitative structure-activity relationships to model t...
High throughput screening experiments are typically used within the pharmaceutical industry for the ...
High throughput screening experiments are typically used within the pharmaceutical industry for the ...
Modern high-throughput screening (HTS) is a well-established approach for hit finding in drug discov...
High Throughput Screening (HTS) is used in drug discovery to screen large numbers of compounds again...
Millions of compounds are available as potential drug candidates. High throughput screening (HTS) is...
High Content Screening (HCS) is a technology that allows life scientists to analyze the effect of bi...
In drug discovery, high content screening (HCS) is an imaging-based method forcell-based screening o...
Background: Computational support for high-content screening (HCS) is of paramount importance at sev...
Complex mixtures containing natural products are still an interesting source of novel drug candidate...
Modern high-throughput screening (HTS) is a well-established approach for hit finding in drug discov...
High-content screening is an empirical strategy in drug discovery toidentify substances capable of a...
Recent technological advances in high-content screening instrumentation have increased its ease of u...
The file attached to this record is the author's final peer reviewed version. The Publisher's final ...
Recent technological advances in high-content screening instrumentation have increased its ease of u...
The versatility of similarity searching and quantitative structure-activity relationships to model t...